Canonical Allele Identifier: CA1104852565
Gene: LMTK2 HGNC NCBI

Linked Data

dbSNP Id: rs1562918546
gnomAD v3: 7-98186857-T-G
gnomAD v4: 7-98186857-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186857T>G , CM000669.2:g.98186857T>G GRCh38
NC_000007.13:g.97816169T>G , CM000669.1:g.97816169T>G GRCh37
NC_000007.12:g.97654105T>G NCBI36
NG_013375.1:g.84973T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.877-20T>G MANE Select ENSP00000297293.5:n.877-20T>G
ENST00000297293.5:c.877-20T>G ENSP00000297293.5:n.877-20T>G
NM_014916.3:c.877-20T>G NP_055731.2:n.877-20T>G
XM_011515981.1:c.871-20T>G XP_011514283.1:n.871-20T>G
XM_011515981.3:c.871-20T>G XP_011514283.1:n.871-20T>G
NM_014916.4:c.877-20T>G MANE Select NP_055731.2:n.877-20T>G
Search 100 bp 5'
Search 100 bp 3'